logging in or signing up 2d nmr bunty_jagiwala Download Post to : URL : Related Presentations : Share Add to Flag Embed Email Send to Blogs and Networks Add to Channel Uploaded from authorPOINT lite Insert YouTube videos in PowerPont slides with aS Desktop Copy embed code: (To copy code, click on the text box) Embed: URL: Thumbnail: WordPress Embed Customize Embed The presentation is successfully added In Your Favorites. Views: 2519 Category: Science & Tech.. License: All Rights Reserved Like it (4) Dislike it (0) Added: October 08, 2009 This Presentation is Public Favorites: 0 Presentation Description No description available. Comments Posting comment... By: KhanBangash (13 month(s) ago) Gr8 Job Buddy Saving..... Post Reply Close Saving..... Edit Comment Close By: bunty_jagiwala (14 month(s) ago) @narugava: can u snd me ur e mail??????????? Saving..... Post Reply Close Saving..... Edit Comment Close By: NARUGAVA (14 month(s) ago) allow me to dld Saving..... Post Reply Close Saving..... Edit Comment Close By: bunty_jagiwala (18 month(s) ago) @edgardov i will send you. Saving..... Post Reply Close Saving..... Edit Comment Close By: naitikthakkar (18 month(s) ago) @edgardov.. tell me ur email id.. i can send u.. naitik Saving..... Post Reply Close Saving..... Edit Comment Close loading.... See all Premium member Presentation Transcript Slide 1: 2D NMR spectroscopy So far we have been dealing with multiple pulses but a single dimension - that is, 1D spectra. We have seen, however, that a multiple pulse sequence can give different spectra which depend on the delay times we use. The ‘basic’ 2D spectrum would involve repeating a multiple pulse 1D sequence with a systematic variation of the delay time tD, and then plotting everything stacked. A very simple example would be varying the time before acquisition (DE): We now have two time domains, one that appears during the acquisition as usual, and one that originates from the variable delay. tD1 tD2 tD3 tDn … … Slide 2: 2D NMR basics There is some renaming that we need to do to be more in synch with the literature: The first perturbation of the system (pulse) will now be called the preparation of the spin system. The variable tD is renamed the evolution time, t1. We have a mixing event, in which information from one part of the spin system is relayed to other parts. Finally, we have an acquisition period (t2) as with all 1D experiments. Schematically, we can draw it like this: t1 is the variable delay time, and t2 is the normal acquisition time. We can envision having f1 and f2, for both frequencies… We’ll see that this format is basically the same for all 2D experiments (and nD, for that matter...). Preparation Evolution Acquisition t1 t2 Mixing Slide 3: A rudimentary 2D experiment We’ll see how it works with the backbone of what will become the COSY pulse sequence. Think of this pulses, were t1 is the preparation time: We’ll analyze it for an off-resonance (wo) singlet for a bunch of different t1 values. Starting after the first p / 2 pulse: 90x 90y t1 t2 y y z x y z x y x x 90x 90x wo wo Slide 4: The rudimentary 2D (continued) The second p / 2 pulse acts only on the y axis component of the magnetization of the <xy> plane. The x axis component is not affected, but its amplitude will depend on the frequency of the line. A(t1) = Ao * cos(wo * t1 ) y y z x y z x y 90x 90x x x wo wo Slide 5: The rudimentary 2D (…) If we plot all the spectra in a stacked plot, we get: Now, we have frequency data in one axis (f2, which came from t2), and time domain data in the other (t1). Since the variation of the amplitude in the t1 domain is also periodic, we can build a pseudo FID if we look at the points for each of the frequencies or lines in f2. One thing that we are overlooking here is that during all the pulsing and waiting and pulsing, the signal will also be affected by T1 and T2 relaxation. wo t1 f2 (t2) t1 A(t1) Slide 6: The rudimentary 2D (…) Now we have FIDs in t1, so we can do a second Fourier transformation in the t1 domain (the first one was in the t2 domain), and obtain a two-dimensional spectrum: • We have a cross-peak where the two lines intercept in the 2D map, in this case on the diagonal. If we had a real spectrum with a lot of signals it would be a royal mess. We look it from above, and draw it as a contour plot. We chop all the peaks with planes at different heights. • Each slice is color-coded depending on the height of the peak. wo wo wo wo f2 f2 f1 f1 Slide 7: The same with some real data This is data from a COSY of pulegone... time - time time - frequency frequency - frequency t2 f2 f2 t1 t1 f1 Slide 8: The same with some real data Now the contour-plot showing all the cross-peaks: OK, were the heck did all the off-diagonal peaks came from, and what do they mean? I’ll do the best I can to explain it, but again, there will be several black-box events. We really need a mathematical description to explain COSY rigorously. f2 f1 Slide 9: Homonuclear correlation - COSY COSY stands for COrrelation SpectroscopY, and for this particular case in which we are dealing with homonuclear couplings, homonuclear correlation spectroscopy. In our development of the 2D idea we considered an isolated spin not coupled to any other spin. Obviously, this is not really useful. What COSY is good for is to tell which spin is connected to which other spin. The off-diagonal peaks are this, and they indicate that those two peaks in the diagonal are coupled. With this basic idea we’ll try to see the effect of the COSY 90y - t1- 90y - t1 pulse sequence on a pair of coupled spins. If we recall the 2 spin-system energy diagram: We see that if we are looking at I and apply both p / 2 pulses, (a pseudo p pulse) we will invert some of the population of spin S, and this will have an effect on I (polarization transfer). I S J (Hz) S S I I • • • • • • • • aIaS aIbS bIaS bIbS Slide 10: Homonuclear correlation (continued) Since the I to S or S to I polarization transfers are the same, we’ll explain it for I to S and assume we get the same for S to I. We first perturb I and analyze what happens to S. After the first p / 2, we have the two I vectors in the x axis, one moving at wI + J / 2 and the other at wI - J / 2. The effect of the second pulse is that it will put the components of the magnetization aligned with y on the -z axis, which means a partial inversion of the I populations. For t1 = 0, we have complete inversion of the I spins (it is a p pulse and the signal intensity of S does not change. For all other times we will have a change on the S intensity that depends periodically on the resonance frequency of I. The variation of the population inversion for I depends on the cosine (or sine) of its resonance frequency. Considering that we are on-resonance with one of the lines and if t1 = 1 / 4 J: y z x y x 90y J / 2 Slide 11: Homonuclear correlation (…) If we do it really general (nothing on-resonance), we would come to this relationship for the change of the S signal (after the p / 2 pulse) as a function of the I resonance frequency and JIS coupling: AS(t1,t2) = Ao * sin( wI * t1 ) * sin (JIS * t1 ) * sin( wS * t2 ) * sin (JIS * t2 ) After Fourier transformation on t1 and t2 , and considering also the I spin, we get: This is the typical pattern for a doublet in a phase-sensitive COSY. The sines make the signals dispersive in f1 and f2. wI wS f1 wS wI f2 Slide 12: Heteronuclear correlation - HETCOR The COSY (or Jenner experiment) was one of the first 2D experiments developed (1971), and is one of the most useful 2D sequences for structural elucidation. There are thousands of variants and improvements (DQF-COSY, E-COSY, etc.). In a similar fashion we can perform a 2D experiment in which we analyze heteronuclear connectivity, that is, which 1H is connected to which 13C. This is called HETCOR, for HETero- nuclear CORrelation spectroscopy. The pulse sequence in this case involves both 13C and 1H, because we have to somehow label the intensities of the 13C with what we do to the populations of 1H. The basic sequence is as follows: 90 {1H} 1H: 13C: 90 90 t1 Slide 13: HETCOR (continued) We first analyze what happens to the 1H proton (that is, we’ll see how the 1H populations are affected), and then see how the 13C signal is affected. For different t1 values we have: y y z x y z x y x x 90 90 y z x y x 90 90, t1 = 0 90, t1 = J / 4 90, t1 = 3J / 4 Slide 14: HETCOR (…) As was the case for COSY, we see that depending on the t1 time we use, we have a variation of the population inversion of the proton. We can clearly see that the amount of inversion depends on the JCH coupling. Although we did it on-resonance for simplicity, we can easily show that it will also depend on the 1H frequency (d). From what we know from SPI and INEPT, we can tell that the periodic variation on the 1H population inversion will have the same periodic effect on the polarization transfer to the 13C. In this case, the two-spin energy diagram is for 1H and 13C: Now, since the intensity of the 13C signal that we detect on t2 is modulated by the frequency of the proton coupled to it, the 13C FID will have information on the 13C and 1H frequencies. aCaH aCbH bCbH 13C 13C 1H 1H bCaH • • • • • • • • • • • • • • • • • • • • 1 4 3 2 1,2 3,4 1,3 2,4 I S Slide 15: HETCOR (…) Again, the intensity of the 13C lines will depend on the 1H population inversion, thus on w1H. If we use a stacked plot for different t1 times, we get: • The intensity of the two 13C lines will vary with the w1H and JCH between +5 and -3 as it did in the INEPT sequence. Mathematically, the intensity of one of the 13C lines from the multiplet will be an equation that depends on w13C on t2 and w1H on t1, as well as JCH on both time domains: A13C(t1, t2) trig(w1Ht1) * trig(w13Ct2 ) * trig(JCHt1) * trig(JCHt2) w13C t1 (w1H) f2 (t2) Slide 16: HETCOR (…) Again, Fourier transformation on both time domains gives us the 2D correlation spectrum, in this case as a contour plot: The main difference in this case is that the 2D spectrum is not symmetrical, because one axis has 13C frequencies and the other 1H frequencies. Pretty cool. Now, we still have the JCH coupling splitting all the signals of the 2D spectrum in little squares. The JCH are in the 50 - 250 Hz range, so we can start having overlap of cross-peaks from different CH spin systems. We’ll see how we can get rid of them without decoupling (if we decouple we won’t see 1H to 13C polarization transfer…). w13C w1H f2 f1 JCH Slide 17: 90 {1H} 1H: 13C: 90 90 t1 HETCOR with no JCH coupling The idea behind it is pretty much the same stuff we did with the refocused INEPT experiment. We use a 13C p pulse to refocus 1H magnetization, and two delays to to maximize polarization transfer from 1H to 13C and to get refocusing of 13C vectors before decoupling. As in INEPT, the effectiveness of the transfer will depend on the delay D and the carbon type. We use an average value. We’ll analyze the case of a methine (CH) carbon... D1 D2 180 t1 / 2 t1 / 2 Slide 18: HETCOR with no JCH coupling (continued) For a certain t1 value, the 1H magnetization behavior is: Now, if we set D1 to 1 / 2J both 1H vectors will dephase by by exactly 180 degrees in this period. This is when we have maximum population inversion for this particular t1, and no JCH effects: x y x y 18013C a b z x b (w1H + J / 2) y a (w1H - J / 2) 90 x y b a t1 / 2 t1 / 2 x y b a z x b y a D1 90 b a Slide 19: HETCOR with no JCH coupling (…) Now we look at the 13C magnetization. After the proton p / 2 we will have the two 13C vectors separated in a 5/3 ratio on the <z> axis. After the second delay D2 (set to 1 / 2J) they will refocus and come together: We can now decouple 1H because the 13C magnetization is refocused. The 2D spectrum now has no JCH couplings (but it still has the chemical shift information), and we just see a single cross-peak where formed by the two chemical shifts: w13C w1H f2 f1 z x 5 y 3 y 3 5 90 y 3 5 D2 x x Slide 23: Long range HETCOR (…) To begin with, D1 and D2 will be in the order of 50 ms instead of 5 ms, which is much longer than before. What will happen now is that antiphase 13C magnetization due to 1JCH couplings will not refocus, and will tend to cancel out. For the 1H part of the refocusing: The delay values are now way of the mark for 1JCH, and we do not have complete inversion of the 1H populations. Now, for the 13C part: At the time we decouple 1H, we will almost kill all the 13C signal that evolved under the effect of 1JCH… x y a b z x b y a D1 90 z x < 5 y < 3 y < 3 < 5 90 y D2 x x Slide 24: Long range HETCOR (…) In the end, we’ll se that most of the magnetization that evolved under the effect of different 1JCHs will be wiped out. On the other hand, 13C antiphase magnetization that originated due to 2JCHwill have the right D1 and D2 delays, so it will behave as we saw before. For 1H: For 13C: So in the end, only 13C that have 2JCH couplings will give rise to correlations in our HETCOR and we will be able to achieve what we wanted x y b a z x b y a D1 (1 / 2 2JCH) 90 z x 5 y 3 y 3 5 90 y 3 5 D2 (1 / 2 2JCH) x x Slide 25: Long range HETCOR (…) If we take our HETCOR using this values for D1 and D2 , and if we consider everything working in our favor, we get: Great. We can now see our long-range 1H-13C coupling, and we can now determine which CH2 carbon is which in camphor. Note that we did the whole explanation for CHs for simplicity, but the picture is pretty much the same for CH2s. As usual, things never go the way we want. This sequence has several drawbacks. First, selecting the right D1 and D2 to see 2JCH over 1JCH is kind of a crap-shot. Second, we are now talking of pretty long delays D1 and D2 on top of the variable evolution delay (which is usually in the order of 10 to 20 ms). We will have a lot of relaxation, not only of the 13C but of the 1H, during this time, and our signal will be pretty weak. Furthermore, since 1H relaxes considerably, the inversion will vanish away and we don’t get strong correlations. Hb Ha Cb Ca Hc a b c Slide 26: COLOC-HETCOR How can we avoid these problems? If we want to keep the idea we have been using, i.e., to refocus 13C magentization associated with 2JCH, we need to keep the D1 and D2 delays. Then the only delay that we could, in principle, make shorter is the variable evolution delay, t1. How do we do this, if we need this delay to vary from experiment to experiment to get the second dimension? The solution is to perform a constant time experiment. This involves to have an evolution time t1 that is overall constant, and equal to D1, but have the pulses inside the evolution progress during this time. The best example of such a pulse sequence is called COrrelations via LOng-range Couplings, or COLOC. The pulse sequence is: 90 {1H} 1H: 13C: 90 90 D2 180 t1 / 2 D1 - t1 / 2 t1 / 2 D1 - t1 / 2 D2 180 D1 Slide 27: COLOC-HETCOR (continued) As you see from the pulse sequence, the D1 period remains the same, as so does the total t1 period. However, we achieve the evolution in t1 by shifting the two 180 pulses through the t1 period constantly from one experiment to the other. We can analyze how this pulse sequence works in the same way we saw how the regular HETCOR works. We’ll see the analysis for a C-C-H. The first 1H 90 puts 1H magnetization in the <xy> plane, were it evolves under the effect of JCH (2JCH in the case of C-C-H) for a period t1 / 2, which is variable. The combination of 180 pulses in 1H and 13C inverts the the 1H magnetization and flips the labels of the 1H vectors: x y a b t1 / 2 x y 18013C 1801H b a ... Slide 28: COLOC-HETCOR (...) Now, after D1 - t1 / 2, the magnetization continues to dephase. However, since the total time is D1, we will get the complete inversion of 1H magnetization, we have the maximum polarization transfer from 1H to 13C, and we tag the 13C magnetization with the 1H frequency (which gives us the correlation…). Since we always have complete inversion of 1H magentization and refocusing, we won’t have 2JCH spliting in the 13C dimension (f1). Finally, over the D2 delay we have refocusing of the 13C antiphase magnetization, just as in the refocused HETCOR, and we can decouple protons during acquisition: The main advantage of this pulse sequence over HETCOR is that we accomplish the same but in a much shorter time, because the D1 period is included in the t1 evolution. Furthermore, instead of increasing t1 from experiment to experiment, we change the relative position of the 180 pulses to achieve the polarization transfer and frequency labeling. z x 5 y 3 y 3 5 90 y 3 5 D2 x x You do not have the permission to view this presentation. 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2d nmr bunty_jagiwala Download Post to : URL : Related Presentations : Share Add to Flag Embed Email Send to Blogs and Networks Add to Channel Uploaded from authorPOINT lite Insert YouTube videos in PowerPont slides with aS Desktop Copy embed code: (To copy code, click on the text box) Embed: URL: Thumbnail: WordPress Embed Customize Embed The presentation is successfully added In Your Favorites. Views: 2519 Category: Science & Tech.. License: All Rights Reserved Like it (4) Dislike it (0) Added: October 08, 2009 This Presentation is Public Favorites: 0 Presentation Description No description available. Comments Posting comment... By: KhanBangash (13 month(s) ago) Gr8 Job Buddy Saving..... Post Reply Close Saving..... Edit Comment Close By: bunty_jagiwala (14 month(s) ago) @narugava: can u snd me ur e mail??????????? Saving..... Post Reply Close Saving..... Edit Comment Close By: NARUGAVA (14 month(s) ago) allow me to dld Saving..... Post Reply Close Saving..... Edit Comment Close By: bunty_jagiwala (18 month(s) ago) @edgardov i will send you. Saving..... Post Reply Close Saving..... Edit Comment Close By: naitikthakkar (18 month(s) ago) @edgardov.. tell me ur email id.. i can send u.. naitik Saving..... Post Reply Close Saving..... Edit Comment Close loading.... See all Premium member Presentation Transcript Slide 1: 2D NMR spectroscopy So far we have been dealing with multiple pulses but a single dimension - that is, 1D spectra. We have seen, however, that a multiple pulse sequence can give different spectra which depend on the delay times we use. The ‘basic’ 2D spectrum would involve repeating a multiple pulse 1D sequence with a systematic variation of the delay time tD, and then plotting everything stacked. A very simple example would be varying the time before acquisition (DE): We now have two time domains, one that appears during the acquisition as usual, and one that originates from the variable delay. tD1 tD2 tD3 tDn … … Slide 2: 2D NMR basics There is some renaming that we need to do to be more in synch with the literature: The first perturbation of the system (pulse) will now be called the preparation of the spin system. The variable tD is renamed the evolution time, t1. We have a mixing event, in which information from one part of the spin system is relayed to other parts. Finally, we have an acquisition period (t2) as with all 1D experiments. Schematically, we can draw it like this: t1 is the variable delay time, and t2 is the normal acquisition time. We can envision having f1 and f2, for both frequencies… We’ll see that this format is basically the same for all 2D experiments (and nD, for that matter...). Preparation Evolution Acquisition t1 t2 Mixing Slide 3: A rudimentary 2D experiment We’ll see how it works with the backbone of what will become the COSY pulse sequence. Think of this pulses, were t1 is the preparation time: We’ll analyze it for an off-resonance (wo) singlet for a bunch of different t1 values. Starting after the first p / 2 pulse: 90x 90y t1 t2 y y z x y z x y x x 90x 90x wo wo Slide 4: The rudimentary 2D (continued) The second p / 2 pulse acts only on the y axis component of the magnetization of the <xy> plane. The x axis component is not affected, but its amplitude will depend on the frequency of the line. A(t1) = Ao * cos(wo * t1 ) y y z x y z x y 90x 90x x x wo wo Slide 5: The rudimentary 2D (…) If we plot all the spectra in a stacked plot, we get: Now, we have frequency data in one axis (f2, which came from t2), and time domain data in the other (t1). Since the variation of the amplitude in the t1 domain is also periodic, we can build a pseudo FID if we look at the points for each of the frequencies or lines in f2. One thing that we are overlooking here is that during all the pulsing and waiting and pulsing, the signal will also be affected by T1 and T2 relaxation. wo t1 f2 (t2) t1 A(t1) Slide 6: The rudimentary 2D (…) Now we have FIDs in t1, so we can do a second Fourier transformation in the t1 domain (the first one was in the t2 domain), and obtain a two-dimensional spectrum: • We have a cross-peak where the two lines intercept in the 2D map, in this case on the diagonal. If we had a real spectrum with a lot of signals it would be a royal mess. We look it from above, and draw it as a contour plot. We chop all the peaks with planes at different heights. • Each slice is color-coded depending on the height of the peak. wo wo wo wo f2 f2 f1 f1 Slide 7: The same with some real data This is data from a COSY of pulegone... time - time time - frequency frequency - frequency t2 f2 f2 t1 t1 f1 Slide 8: The same with some real data Now the contour-plot showing all the cross-peaks: OK, were the heck did all the off-diagonal peaks came from, and what do they mean? I’ll do the best I can to explain it, but again, there will be several black-box events. We really need a mathematical description to explain COSY rigorously. f2 f1 Slide 9: Homonuclear correlation - COSY COSY stands for COrrelation SpectroscopY, and for this particular case in which we are dealing with homonuclear couplings, homonuclear correlation spectroscopy. In our development of the 2D idea we considered an isolated spin not coupled to any other spin. Obviously, this is not really useful. What COSY is good for is to tell which spin is connected to which other spin. The off-diagonal peaks are this, and they indicate that those two peaks in the diagonal are coupled. With this basic idea we’ll try to see the effect of the COSY 90y - t1- 90y - t1 pulse sequence on a pair of coupled spins. If we recall the 2 spin-system energy diagram: We see that if we are looking at I and apply both p / 2 pulses, (a pseudo p pulse) we will invert some of the population of spin S, and this will have an effect on I (polarization transfer). I S J (Hz) S S I I • • • • • • • • aIaS aIbS bIaS bIbS Slide 10: Homonuclear correlation (continued) Since the I to S or S to I polarization transfers are the same, we’ll explain it for I to S and assume we get the same for S to I. We first perturb I and analyze what happens to S. After the first p / 2, we have the two I vectors in the x axis, one moving at wI + J / 2 and the other at wI - J / 2. The effect of the second pulse is that it will put the components of the magnetization aligned with y on the -z axis, which means a partial inversion of the I populations. For t1 = 0, we have complete inversion of the I spins (it is a p pulse and the signal intensity of S does not change. For all other times we will have a change on the S intensity that depends periodically on the resonance frequency of I. The variation of the population inversion for I depends on the cosine (or sine) of its resonance frequency. Considering that we are on-resonance with one of the lines and if t1 = 1 / 4 J: y z x y x 90y J / 2 Slide 11: Homonuclear correlation (…) If we do it really general (nothing on-resonance), we would come to this relationship for the change of the S signal (after the p / 2 pulse) as a function of the I resonance frequency and JIS coupling: AS(t1,t2) = Ao * sin( wI * t1 ) * sin (JIS * t1 ) * sin( wS * t2 ) * sin (JIS * t2 ) After Fourier transformation on t1 and t2 , and considering also the I spin, we get: This is the typical pattern for a doublet in a phase-sensitive COSY. The sines make the signals dispersive in f1 and f2. wI wS f1 wS wI f2 Slide 12: Heteronuclear correlation - HETCOR The COSY (or Jenner experiment) was one of the first 2D experiments developed (1971), and is one of the most useful 2D sequences for structural elucidation. There are thousands of variants and improvements (DQF-COSY, E-COSY, etc.). In a similar fashion we can perform a 2D experiment in which we analyze heteronuclear connectivity, that is, which 1H is connected to which 13C. This is called HETCOR, for HETero- nuclear CORrelation spectroscopy. The pulse sequence in this case involves both 13C and 1H, because we have to somehow label the intensities of the 13C with what we do to the populations of 1H. The basic sequence is as follows: 90 {1H} 1H: 13C: 90 90 t1 Slide 13: HETCOR (continued) We first analyze what happens to the 1H proton (that is, we’ll see how the 1H populations are affected), and then see how the 13C signal is affected. For different t1 values we have: y y z x y z x y x x 90 90 y z x y x 90 90, t1 = 0 90, t1 = J / 4 90, t1 = 3J / 4 Slide 14: HETCOR (…) As was the case for COSY, we see that depending on the t1 time we use, we have a variation of the population inversion of the proton. We can clearly see that the amount of inversion depends on the JCH coupling. Although we did it on-resonance for simplicity, we can easily show that it will also depend on the 1H frequency (d). From what we know from SPI and INEPT, we can tell that the periodic variation on the 1H population inversion will have the same periodic effect on the polarization transfer to the 13C. In this case, the two-spin energy diagram is for 1H and 13C: Now, since the intensity of the 13C signal that we detect on t2 is modulated by the frequency of the proton coupled to it, the 13C FID will have information on the 13C and 1H frequencies. aCaH aCbH bCbH 13C 13C 1H 1H bCaH • • • • • • • • • • • • • • • • • • • • 1 4 3 2 1,2 3,4 1,3 2,4 I S Slide 15: HETCOR (…) Again, the intensity of the 13C lines will depend on the 1H population inversion, thus on w1H. If we use a stacked plot for different t1 times, we get: • The intensity of the two 13C lines will vary with the w1H and JCH between +5 and -3 as it did in the INEPT sequence. Mathematically, the intensity of one of the 13C lines from the multiplet will be an equation that depends on w13C on t2 and w1H on t1, as well as JCH on both time domains: A13C(t1, t2) trig(w1Ht1) * trig(w13Ct2 ) * trig(JCHt1) * trig(JCHt2) w13C t1 (w1H) f2 (t2) Slide 16: HETCOR (…) Again, Fourier transformation on both time domains gives us the 2D correlation spectrum, in this case as a contour plot: The main difference in this case is that the 2D spectrum is not symmetrical, because one axis has 13C frequencies and the other 1H frequencies. Pretty cool. Now, we still have the JCH coupling splitting all the signals of the 2D spectrum in little squares. The JCH are in the 50 - 250 Hz range, so we can start having overlap of cross-peaks from different CH spin systems. We’ll see how we can get rid of them without decoupling (if we decouple we won’t see 1H to 13C polarization transfer…). w13C w1H f2 f1 JCH Slide 17: 90 {1H} 1H: 13C: 90 90 t1 HETCOR with no JCH coupling The idea behind it is pretty much the same stuff we did with the refocused INEPT experiment. We use a 13C p pulse to refocus 1H magnetization, and two delays to to maximize polarization transfer from 1H to 13C and to get refocusing of 13C vectors before decoupling. As in INEPT, the effectiveness of the transfer will depend on the delay D and the carbon type. We use an average value. We’ll analyze the case of a methine (CH) carbon... D1 D2 180 t1 / 2 t1 / 2 Slide 18: HETCOR with no JCH coupling (continued) For a certain t1 value, the 1H magnetization behavior is: Now, if we set D1 to 1 / 2J both 1H vectors will dephase by by exactly 180 degrees in this period. This is when we have maximum population inversion for this particular t1, and no JCH effects: x y x y 18013C a b z x b (w1H + J / 2) y a (w1H - J / 2) 90 x y b a t1 / 2 t1 / 2 x y b a z x b y a D1 90 b a Slide 19: HETCOR with no JCH coupling (…) Now we look at the 13C magnetization. After the proton p / 2 we will have the two 13C vectors separated in a 5/3 ratio on the <z> axis. After the second delay D2 (set to 1 / 2J) they will refocus and come together: We can now decouple 1H because the 13C magnetization is refocused. The 2D spectrum now has no JCH couplings (but it still has the chemical shift information), and we just see a single cross-peak where formed by the two chemical shifts: w13C w1H f2 f1 z x 5 y 3 y 3 5 90 y 3 5 D2 x x Slide 23: Long range HETCOR (…) To begin with, D1 and D2 will be in the order of 50 ms instead of 5 ms, which is much longer than before. What will happen now is that antiphase 13C magnetization due to 1JCH couplings will not refocus, and will tend to cancel out. For the 1H part of the refocusing: The delay values are now way of the mark for 1JCH, and we do not have complete inversion of the 1H populations. Now, for the 13C part: At the time we decouple 1H, we will almost kill all the 13C signal that evolved under the effect of 1JCH… x y a b z x b y a D1 90 z x < 5 y < 3 y < 3 < 5 90 y D2 x x Slide 24: Long range HETCOR (…) In the end, we’ll se that most of the magnetization that evolved under the effect of different 1JCHs will be wiped out. On the other hand, 13C antiphase magnetization that originated due to 2JCHwill have the right D1 and D2 delays, so it will behave as we saw before. For 1H: For 13C: So in the end, only 13C that have 2JCH couplings will give rise to correlations in our HETCOR and we will be able to achieve what we wanted x y b a z x b y a D1 (1 / 2 2JCH) 90 z x 5 y 3 y 3 5 90 y 3 5 D2 (1 / 2 2JCH) x x Slide 25: Long range HETCOR (…) If we take our HETCOR using this values for D1 and D2 , and if we consider everything working in our favor, we get: Great. We can now see our long-range 1H-13C coupling, and we can now determine which CH2 carbon is which in camphor. Note that we did the whole explanation for CHs for simplicity, but the picture is pretty much the same for CH2s. As usual, things never go the way we want. This sequence has several drawbacks. First, selecting the right D1 and D2 to see 2JCH over 1JCH is kind of a crap-shot. Second, we are now talking of pretty long delays D1 and D2 on top of the variable evolution delay (which is usually in the order of 10 to 20 ms). We will have a lot of relaxation, not only of the 13C but of the 1H, during this time, and our signal will be pretty weak. Furthermore, since 1H relaxes considerably, the inversion will vanish away and we don’t get strong correlations. Hb Ha Cb Ca Hc a b c Slide 26: COLOC-HETCOR How can we avoid these problems? If we want to keep the idea we have been using, i.e., to refocus 13C magentization associated with 2JCH, we need to keep the D1 and D2 delays. Then the only delay that we could, in principle, make shorter is the variable evolution delay, t1. How do we do this, if we need this delay to vary from experiment to experiment to get the second dimension? The solution is to perform a constant time experiment. This involves to have an evolution time t1 that is overall constant, and equal to D1, but have the pulses inside the evolution progress during this time. The best example of such a pulse sequence is called COrrelations via LOng-range Couplings, or COLOC. The pulse sequence is: 90 {1H} 1H: 13C: 90 90 D2 180 t1 / 2 D1 - t1 / 2 t1 / 2 D1 - t1 / 2 D2 180 D1 Slide 27: COLOC-HETCOR (continued) As you see from the pulse sequence, the D1 period remains the same, as so does the total t1 period. However, we achieve the evolution in t1 by shifting the two 180 pulses through the t1 period constantly from one experiment to the other. We can analyze how this pulse sequence works in the same way we saw how the regular HETCOR works. We’ll see the analysis for a C-C-H. The first 1H 90 puts 1H magnetization in the <xy> plane, were it evolves under the effect of JCH (2JCH in the case of C-C-H) for a period t1 / 2, which is variable. The combination of 180 pulses in 1H and 13C inverts the the 1H magnetization and flips the labels of the 1H vectors: x y a b t1 / 2 x y 18013C 1801H b a ... Slide 28: COLOC-HETCOR (...) Now, after D1 - t1 / 2, the magnetization continues to dephase. However, since the total time is D1, we will get the complete inversion of 1H magnetization, we have the maximum polarization transfer from 1H to 13C, and we tag the 13C magnetization with the 1H frequency (which gives us the correlation…). Since we always have complete inversion of 1H magentization and refocusing, we won’t have 2JCH spliting in the 13C dimension (f1). Finally, over the D2 delay we have refocusing of the 13C antiphase magnetization, just as in the refocused HETCOR, and we can decouple protons during acquisition: The main advantage of this pulse sequence over HETCOR is that we accomplish the same but in a much shorter time, because the D1 period is included in the t1 evolution. Furthermore, instead of increasing t1 from experiment to experiment, we change the relative position of the 180 pulses to achieve the polarization transfer and frequency labeling. z x 5 y 3 y 3 5 90 y 3 5 D2 x x